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As the inflammation in those types of demyelinating disorders is complex and engages varied types of effector cells, ranging from plasma cells and T CD4 + cells to astrocytes and microglia, the most promising potential medications shall possess pleiotropic, multi-faceted anti-inflammatory capabilities to effectively counteract immunological response to organisms own myelin elements and other cell fractions associated with them [34]

Bisphenol A induced oxidative stress mediated genotoxicity in Drosophila melanogaster

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